Biblio

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2024
Odabas GPelin, Aslan K, Suna PAlisan, Kendirli PKader, Erdem S, Cakir M, Ozcan A, Yilmaz E, Karakukcu M, Donmez-Altuntas H, et al. Alantolactone ameliorates graft versus host disease in mice. Int Immunopharmacol. 2024;128:111560.
Lanz A-L, Erdem S, Ozcan A, Ceylaner G, Cansever M, Ceylaner S, Conca R, Magg T, Acuto O, Latour S, et al. Correction to: A Novel Biallelic LCK Variant Resulting in Profound T-Cell Immune Deficiency and Review of the Literature. J Clin Immunol. 2024;44(1):41.
Isik E, Aydinok Y, Albayrak C, Durmus B, Karakas Z, Orhan MFatih, Sarper N, Aydın S, Unal S, Oymak Y, et al. Identification of the molecular etiology in rare congenital hemolytic anemias using next-generation sequencing with exome-based copy number variant analysis. Eur J Haematol. 2024.
2023
Ozcelik F, Aslan K, Gok V, Ari MBilgehan, Ozcan A, Eken A, Unal E, Ozkul Y, Dundar M. A case of autoimmune lymphoproliferative syndrome with a novel variant. Pediatr Hematol Oncol. 2023:1-9.
Erdem S, Haskoloğlu Ş, Haliloglu Y, Çelikzencir H, Arik E, Keskin O, Eltan SBilgic, Yucel E, Canatan H, Avcilar H, et al. Defective Treg generation and increased type 3 immune response in leukocyte adhesion deficiency 1. Clin Immunol. 2023:109691.
Lanz A-L, Erdem S, Ozcan A, Ceylaner G, Cansever M, Ceylaner S, Conca R, Magg T, Acuto O, Latour S, et al. A Novel Biallelic LCK Variant Resulting in Profound T-Cell Immune Deficiency and Review of the Literature. J Clin Immunol. 2023;44(1):1.
2022
Gok V, Ozcan A, Ozer S, Karaman F, Aykutlu E, Yilmaz E, Karakukcu M, Bisgin A, Unal E. Aceruloplasminemia presenting with microcytic anemia in a Turkish boy due to a novel pathogenic variant. Pediatr Hematol Oncol. 2022:1-9.
Kondolot M, Yilmaz E, Sahin NErdog, Ozcan A, Kaynar L, Unal E, Karakukcu M. ANTIBODY RESPONSE AGAINST VACCINE ANTIGENS IN CHILDREN AFTER TCRαβ DEPLETED HAPLOIDENTICAL STEM CELL TRANSPLANTATION: IS IT SIMILAR TO RECIPIENTS WHO HAVE FULL-MATCHED DONORS. Transplant Cell Ther. 2022.
Samur BM, Samur TG, Çiflikli F-E, Ozcan A, Gok V, Soykan R, Soytürk F, Kılıç Ö, Kandur M, Kandemir R, et al. Evaluation of primary care physicians' approaches to hemophilia and bleeding disorders: a questionnaire survey. Blood Coagul Fibrinolysis. 2022.
Gok V, Erdem S, Haliloglu Y, Bisgin A, Belkaya S, Başaran KErdem, Canatan MFatih, Ozcan A, Yilmaz E, Acıpayam C, et al. Immunodeficiency associated with a novel functionally defective variant of SLC19A1 benefits from folinic acid treatment. Genes Immun. 2022.
Leiding JW, Vogel TP, Santarlas VGJ, Mhaskar R, Smith MR, Carisey A, Vargas-Hernández A, Silva-Carmona M, Heeg M, Rensing-Ehl A, et al. Monogenic Early-Onset Lymphoproliferation and Autoimmunity: The Natural History of STAT3 GOF Syndrome. J Allergy Clin Immunol. 2022.
Alsavaf MBilal, Verboon JM, Dogan ME, Azizoglu ZBusra, Okus FZehra, Ozcan A, Dundar M, Eken A, Donmez-Altuntas H, Sankaran VG, et al. A novel missense mutation outside the DNAJ domain of DNAJC21 is associated with Shwachman-Diamond syndrome. Br J Haematol. 2022.
Gok V, Tada H, Dogan MEnsar, Sari UAlakus, Aslan K, Ozcan A, Yilmaz E, Kardas F, Karakukcu M, Canatan H, et al. A teenager boy with a novel variant of Sitosterolemia presented with pancytopenia. Clin Chim Acta. 2022.